52421-48-4 Usage
Description
DL-N-BENZOYL-2-BENZYLSERINE is a chemical compound that belongs to the class of benzoyl amino acids. It is a derivative of benzoylserine, which is a naturally occurring amino acid found in proteins. DL-N-BENZOYL-2-BENZYLSERINE is characterized by its potential applications in pharmaceutical research and development, where it serves as a building block in the synthesis of various compounds.
Uses
Used in Pharmaceutical Research and Development:
DL-N-BENZOYL-2-BENZYLSERINE is used as a building block for the synthesis of various compounds, contributing to the advancement of medicinal chemistry and drug discovery. Its role in the creation of new pharmaceuticals is significant, as it may be a key component in developing innovative treatments and therapies.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, DL-N-BENZOYL-2-BENZYLSERINE is utilized for its potential to contribute to the understanding of biochemical pathways and processes. Its unique structure and properties make it a valuable tool for studying and manipulating biological systems at the molecular level.
Used in Drug Discovery:
DL-N-BENZOYL-2-BENZYLSERINE holds promise in drug discovery due to its potential therapeutic properties. Researchers are interested in further investigating this compound to explore its capabilities in the development of new drugs that could address a variety of health conditions and diseases.
Overall, DL-N-BENZOYL-2-BENZYLSERINE is a versatile compound with applications across multiple sectors within the pharmaceutical industry, from basic research to the development of novel therapeutic agents. Its potential impact on medicine and healthcare is substantial, warranting continued exploration and investment in its study and application.
Check Digit Verification of cas no
The CAS Registry Mumber 52421-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,2 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52421-48:
(7*5)+(6*2)+(5*4)+(4*2)+(3*1)+(2*4)+(1*8)=94
94 % 10 = 4
So 52421-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H17NO4/c19-12-17(16(21)22,11-13-7-3-1-4-8-13)18-15(20)14-9-5-2-6-10-14/h1-10,19H,11-12H2,(H,18,20)(H,21,22)/p-1/t17-/m1/s1
52421-48-4Relevant articles and documents
Optical resolution by preferential crystallization of (RS)-2-benzoylamino-2-benzyl-3-hydroxypropanoic acid and its use in synthesizing optically active 2-amino-2-methyl-3-phenylpropanoic acid.
Shiraiwa, Tadashi,Suzuki, Masahiro,Sakai, Yoshio,Nagasawa, Hisashi,Takatani, Kazuhiro,Noshi, Daisuke,Yamanashi, Kenji
, p. 1362 - 1366 (2007/10/03)
To synthesize optically active 2-amino-2-methyl-3-phenylpropanoic acid (1), (RS)-2-benzoylamino-2-benzyl-3-hydroxypropanoic acid [(RS)-2] was first optically resolved using cinchonidine as a resolving agent to yield optically pure (S)- and (R)-2 in yields of about 70%, based on half of the starting amount of (RS)-2. Next, the racemic structure of (RS)-2 was examined based on melting point, solubility, IR spectrum, and binary and ternary phase diagrams, with the aim of optical resolution by preferential crystallization of (RS)-2. Results indicated that the (RS)-2 exists as a conglomerate at room temperature, although it forms a racemic compound at the melting point. The optical resolution by preferential crystallization yielded (S)- and (R)-2 with optical purities of about 90%, which were fully purified by recrystallization. After O-tosylation of (S)- and (R)-2, reduction by zinc powder and sodium iodide gave (R)- and (S)-1, respectively.
